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Process Development Engineer

Job in 3400, Burgdorf, Canton de Berne, Switzerland
Listing for: mylife Diabetes Care
Full Time position
Listed on 2026-05-29
Job specializations:
  • Engineering
    Manufacturing Engineer, Process Engineer, Quality Engineering, Medical Device Industry
  • Manufacturing / Production
    Manufacturing Engineer, Quality Engineering, Medical Device Industry
Salary/Wage Range or Industry Benchmark: 80000 - 100000 CHF Yearly CHF 80000.00 100000.00 YEAR
Job Description & How to Apply Below

We are looking for a hands-on Process Development Engineer to help industrialize and scale up medical device consumables. You will own process development, design transfer, and manufacturing optimisation together with our contract manufacturers (CMOs) in Europe and Central America. The work is cross-functional, the environment is growing fast, and the role comes with real ownership over how things get built.

Your goal is to establish production processes that are robust, scalable, and cost-efficient. You will work independently, travel regularly (30-40% international), and collaborate closely with Quality, Operations, Supply Chain, R&D, and external suppliers. This is a technical role where problem-solving matters more than presentations.

Your main Tasks

  • Lead and support design transfer activities to external manufacturing partners (CMOs), including product and engineering changes
  • Optimize and scale manufacturing and assembly processes for medical device consumables in collaboration with external manufacturing partners
  • Support process validation activities (IQ/OQ/PQ), equipment qualification, and manufacturing readiness
  • Identify and implement process and automation improvements to increase robustness, reduce manufacturing risks, and improve efficiency
  • Collaborate closely with suppliers and cross-functional teams including Quality, Operations, Supply Chain, and R&D

Your profile

  • Degree in Production Engineering, Mechanical Engineering, Medical Engineering, or similar technical field
  • 5–10 years of experience in process development, industrialization, manufacturing engineering, or design transfer within Med Tech, preferably in plastic part assembly and consumable manufacturing
  • Knowledge of medical device production standards, sterilization processes and regulated manufacturing environments
  • Independent and structured working style with strong ownership mindset
  • Fluent in English;
    German and/or Spanish are considered a plus
  • Willingness to travel internationally (30–40%)
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